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| | ==Crystal structure of the pyruvate kinase (PK1) from the mosquito Aedes aegypti== | | ==Crystal structure of the pyruvate kinase (PK1) from the mosquito Aedes aegypti== |
| - | <StructureSection load='6du6' size='340' side='right' caption='[[6du6]], [[Resolution|resolution]] 3.51Å' scene=''> | + | <StructureSection load='6du6' size='340' side='right'caption='[[6du6]], [[Resolution|resolution]] 3.51Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[6du6]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Aedae Aedae]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DU6 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6DU6 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6du6]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Aedes_aegypti Aedes aegypti]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DU6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6DU6 FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=FBP:BETA-FRUCTOSE-1,6-DIPHOSPHATE'>FBP</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.513Å</td></tr> |
| - | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">5565629, AAEL014913 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=7159 AEDAE])</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FBP:BETA-FRUCTOSE-1,6-DIPHOSPHATE'>FBP</scene></td></tr> |
| - | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Pyruvate_kinase Pyruvate kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.40 2.7.1.40] </span></td></tr>
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6du6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6du6 OCA], [https://pdbe.org/6du6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6du6 RCSB], [https://www.ebi.ac.uk/pdbsum/6du6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6du6 ProSAT]</span></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6du6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6du6 OCA], [http://pdbe.org/6du6 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6du6 RCSB], [http://www.ebi.ac.uk/pdbsum/6du6 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6du6 ProSAT]</span></td></tr> | + | |
| | </table> | | </table> |
| | + | == Function == |
| | + | [https://www.uniprot.org/uniprot/Q16F38_AEDAE Q16F38_AEDAE] |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | </div> | | </div> |
| | <div class="pdbe-citations 6du6" style="background-color:#fffaf0;"></div> | | <div class="pdbe-citations 6du6" style="background-color:#fffaf0;"></div> |
| | + | |
| | + | ==See Also== |
| | + | *[[Pyruvate kinase 3D structures|Pyruvate kinase 3D structures]] |
| | == References == | | == References == |
| | <references/> | | <references/> |
| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Aedae]] | + | [[Category: Aedes aegypti]] |
| - | [[Category: Pyruvate kinase]] | + | [[Category: Large Structures]] |
| - | [[Category: Murillo-Solano, C]] | + | [[Category: Murillo-Solano C]] |
| - | [[Category: Petchampai, N]] | + | [[Category: Petchampai N]] |
| - | [[Category: Pizarro, J C]] | + | [[Category: Pizarro JC]] |
| - | [[Category: Scaraffia, P Y]] | + | [[Category: Scaraffia PY]] |
| - | [[Category: Carbon metabolism]]
| + | |
| - | [[Category: Glycolysis]]
| + | |
| - | [[Category: Mosquito]]
| + | |
| - | [[Category: Transferase]]
| + | |
| - | [[Category: Vector]]
| + | |
| Structural highlights
Function
Q16F38_AEDAE
Publication Abstract from PubMed
Female Aedes aegypti mosquitoes are vectors of arboviruses that cause diseases of public health significance. The discovery of new metabolic targets is crucial for improving mosquito control strategies. We recently demonstrated that glucose oxidation supports ammonia detoxification in Aedes aegypti. Pyruvate kinase (PK, EC 2.7.1.40) catalyzes the last step of the glycolytic pathway. In most organisms, one or more allosteric effectors control PK activity. However, the kinetic properties and structure of PK in mosquitoes have not been previously reported. In this study, two alternatively spliced mRNA variants (AaPK1 and AaPK2) that code for PKs were identified in the A. aegypti genome. The AaPK1 mRNA variant, which encodes a 529 amino acid protein with an estimated molecular weight of approximately 57kDa, was cloned. The protein was expressed in Escherichia coli and purified. The AaPK1 kinetic properties were identified. The recombinant protein was also crystallized and its 3D structure determined. We found that alanine, glutamine, proline, serine and fructose-1-phosphate displayed a classic allosteric activation on AaPK1. Ribulose-5-phosphate acted as an allosteric inhibitor of AaPK1 but its inhibitory effect was reversed by alanine, glutamine, proline and serine. Additionally, the allosteric activation of AaPK1 by amino acids was weakened by fructose-1,6-bisphosphate, whereas the allosteric activation of AaPK1 by alanine and serine was diminished by glucose-6-phosphate. The AaPK1 structure shows the presence of fructose-1,6-bisphosphate in the allosteric site. Together, our results reveal that specific amino acids and phosphorylated sugars tightly regulate conformational dynamics and catalytic changes of AaPK1. The distinctive AaPK1 allosteric properties support a complex role for this enzyme within mosquito metabolism.
Distinctive regulatory properties of pyruvate kinase 1 from Aedes aegypti mosquitoes.,Petchampai N, Murillo-Solano C, Isoe J, Pizarro JC, Scaraffia PY Insect Biochem Mol Biol. 2018 Dec 19. pii: S0965-1748(18)30450-8. doi:, 10.1016/j.ibmb.2018.12.010. PMID:30578824[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Petchampai N, Murillo-Solano C, Isoe J, Pizarro JC, Scaraffia PY. Distinctive regulatory properties of pyruvate kinase 1 from Aedes aegypti mosquitoes. Insect Biochem Mol Biol. 2018 Dec 19. pii: S0965-1748(18)30450-8. doi:, 10.1016/j.ibmb.2018.12.010. PMID:30578824 doi:http://dx.doi.org/10.1016/j.ibmb.2018.12.010
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